Combined Interleukin‐12 and Topical Chemotherapy for Established Leishmaniasis Drastically Reduces Tissue Parasitism and Relapses in Susceptible Mice
Author(s) -
Ana Paula Fernandes,
Fernando Aécio de Amorim Carvalho,
Carlos Alberto Pereira Tavares,
Helton C. Santiago,
Gisele A. Castro,
Wagner Luiz Tafuri,
Lucas Antônio Miranda Ferreira,
Ricardo T. Gazzinelli
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/320699
Subject(s) - paromomycin , immunology , chemotherapy , leishmaniasis , medicine , cytokine , cutaneous leishmaniasis , interferon gamma , interleukin 2 , biology , antibiotics , microbiology and biotechnology , aminoglycoside
The efficacy of the association of paromomycin sulfate (PA) with recombinant (r) interleukin (IL)-12 was investigated by topical treatment of BALB/c mice infected with Leishmania major that displayed fully developed cutaneous lesions. Although healing was observed in PA-treated groups, lesions recurred in 100% of these animals 70 days after treatment. In contrast, lesions were absent in a high proportion of PA- and rIL-12-treated mice 120 days after treatment. The PA/rIL-12-treated mice had a switch in cytokine response, from high IL-4 and low interferon (IFN)-gamma levels to low IL-4 and high IFN-gamma levels, and reductions in parasite load, dissemination of parasites, and inflammation. Thus, the association of rIL-12 to topical chemotherapy for leishmaniasis may be an important strategy for increasing cure rates and decreasing the incidence of relapse.
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